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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1154974Erstellt: 25. Oktober 2026

Isobutylamine → 7-amino-2,2-dimethyl-8-(2-methylpropyl)-6-nitroso-3H-imidazo[1,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/1154974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutylamineHCID 6558—
EduktSodium HydroxideHCID 14798—
Edukt4-ChlorobenzylamineHCID 66036—
EduktSodium dithionateHCID 146045—
EduktEthyl 2-cyano-2-(hydroxyimino)acetateHCID 6399078—
EduktHCID 178448423HCID 178448423—
Edukt2-Methylthio-4,4-dimethyl-2-imidazoline hydrochlorideHCID 178503443—
LösungsmittelFormic AcidHCID 284—
Produkt7-amino-2,2-dimethyl-8-(2-methylpropyl)-6-nitroso-3H-imidazo[1,2-a]pyrimidin-5-oneHCID 178448424—

Reaktionsschritte

6,7-DIHYDRO-4-(2METHYLPROPYL)-6,6-DIMETHYL-3H-IMIDAZO[1,2-a]PURIN-9(4H)-ONE.-- 7-Amino-2,3-dihydro-2,2-dimethyl-8-(2-methylpropyl)-6-nitrosoimidazo[1,2-a]pyrimidin-5(8H)-one was prepared by reaction of the 2-methylthio-4,4-dimethyl-2-imidazoline hydrochloride with 2-methylpropylamine according to the method of Procedure 103 by substitution of the latter for p-chlorobenzylamine. The reaction product from this step was then condensed with ethyl oximinocyanoacetate as described in Procedure 103. The resulting nitroso compound was then reduced with sodium dithionate in formic acid and the resulting formylamino compound was cyclized with dilute aqueous sodium hydroxide according to Procedure 100.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04298734
Quelldatensatzuspto-grants-1981_11
ORD IDord-919ec093ce254ff6b83298a0c56dee4c
Quellennotizuspto-grants-1981_11